Evidence map›Paper›PMID 40377871›Full record

ReviewProbiotics and antimicrobial proteins2026

CRISPR-Assisted Probiotic and In Situ Engineering of Gut Microbiota: A Prospect to Modification of Metabolic Disorders.

Rahem Rahmati, Fatemeh Zarimeidani, Mohammad Reza Ghanbari Boroujeni, Sepideh Sadighbathi, Zeinab Kashaniasl, Mobina Saleh, Iraj Alipourfard

Abstract readReview
In one paragraph

Review in Probiotics and antimicrobial proteins, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

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  8. Foods (Basel, Switzerland) · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Rahem RahmatiStudents Research Committee, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Fatemeh ZarimeidaniStudents Research Committee, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Mohammad Reza Ghanbari BoroujeniStudents Research Committee, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Sepideh SadighbathiDepartment of Comparative Biomedicine and Food Science, University of Padua, Padua, Italy.
Zeinab KashaniaslCollege of Pharmacy, Department of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA.
Mobina SalehStudents Research Committee, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Iraj AlipourfardInstitute of Physical Chemistry, Polish Academy of Sciences, Marcina Kasprzaka 44/52, 01-224, Warsaw, Poland. ialipourfard@ichf.edu.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiota, a substantial group of microorganisms residing in the human body, profoundly impacts various physiological and pathological mechanisms. Recent studies have elucidated the association between gut dysbiosis and multiple organ diseases. Gut microbiota plays a crucial role in maintaining gastrointestinal stability, regulating the immune system and metabolic processes not only within the gastrointestinal tract but also in other organs such as the brain, lungs, and skin. Dysbiosis of the gut microbiota can disrupt biological functioning and contribute to the development of metabolic disorders. The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and CRISPR-associated proteins (Cas) modules are adaptive immune systems in numerous archaea and bacteria. CRISPR/Cas is a versatile gene-editing tool that enables modification of the genome in live cells, including those within the gut microbiota. This technique has revolutionized gene editing due to its simplicity and effectiveness. It finds extensive applications in diverse scientific arenas, facilitating the functional screening of genomes during various biological processes. Additionally, CRISPR has been instrumental in creating model organisms and cell lines for research purposes and holds great potential for developing personalized medical treatments through precise genetic alterations. This review aims to explore and discuss the possibilities of CRISPR/Cas and the current trends in using this technique for editing gut microbiota genes in various metabolic disorders. By uncovering the valuable potential of CRISPR/Cas in modifying metabolic disorders through the human gut microbiota, we shed light on its promising applications.

Indexed as

CRISPR-Cas SystemsGastrointestinal MicrobiomeGene EditingMetabolic DiseasesProbioticsAnimalsClustered Regularly Interspaced Short Palindromic RepeatsHumansCRISPRFMTMetabolic disordersMicrobiomeProbiotics

Identifiers

PMID40377871
PMCPMC12999876

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.